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Wioletta Krysa
Observed names:
Krysa, Wioletta,
W Krysa,
W. Krysa
Institution:
Institute of Psychiatry and Neurology
Observed institutions:
Medical University of Warsaw,
Institute of Psychiatry and Neurology
OpenAlex ID:
A5009727395
CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion
2012
·
J.-M. Lee
, E.M. Ramos
, et al.
·
Neurology
·
382
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study
2017
·
Davina J Hensman Moss
, Antonio F Pardiñas
, et al.
·
The Lancet Neurology
·
311
PDF
Self-awareness of Motor Dysfunction in Patients with Huntington's Disease in Comparison to Parkinson's Disease and Cervical Dystonia
2011
·
Emilia J. Sitek
, Witold Sołtan
, et al.
·
Journal of the International Neuropsychological Society
·
71
Clinical manifestations of intermediate allele carriers in Huntington disease
2016
·
Esther Cubo
, María A. Ramos-Arroyo
, et al.
·
Neurology
·
53
Next-generation sequencing study reveals the broader variant spectrum of hereditary spastic paraplegia and related phenotypes
2019
·
Ewelina Elert-Dobkowska
, Iwona Stepniak
, et al.
·
Neurogenetics
·
47
PDF
Reduced Cancer Incidence in Huntington’s Disease: Analysis in the Registry Study
2018
·
Paul McNulty
, Richard Pilcher
, et al.
·
Journal of Huntington s Disease
·
35
Molecular spectrum of the SPAST, ATL1 and REEP1 gene mutations associated with the most common hereditary spastic paraplegias in a group of Polish patients
2015
·
Ewelina Elert-Dobkowska
, Iwona Stepniak
, et al.
·
Journal of the Neurological Sciences
·
33
Screening for the hereditary spastic paraplaegias SPG4 and SPG3A with the multiplex ligation-dependent probe amplification technique in a large population of affected individuals
2011
·
Anna Sulek
, Ewelina Elert
, et al.
·
Neurological Sciences
·
30
The occurrence of spinocerebellar ataxias caused by dynamic mutations in Polish patients
2010
·
Anna Sułek-Piątkowska
, Elżbieta Zdzienicka
, et al.
·
Neurologia i Neurochirurgia Polska
·
24
PDF
Muscle pathology in myotonic dystrophy: light and electron microscopic investigation in eighteen patients.
2011
·
A Nadaj-Pakleza
, A Lusakowska
, et al.
·
PubMed
·
23
PDF
High relative frequency of SCA1 in Poland reflecting a potential founder effect
2016
·
Wioletta Krysa
, Anna Sulek
, et al.
·
Neurological Sciences
·
20
PDF
The personal experience of parenting a child with Juvenile Huntington’s Disease: perceptions across Europe
2013
·
Virginia Eatough
, Helen Santini
, et al.
·
European Journal of Human Genetics
·
20
PDF
Rapid detection of large expansions in progressive myoclonus epilepsy type 1, myotonic dystrophy type 2 and spinocerebellar ataxia type 8
2012
·
Wioletta Krysa
, Marta Rajkiewicz
, et al.
·
Neurologia i Neurochirurgia Polska
·
13
Searching for mutation in the JPH3, ATN1 and TBP genes in Polish patients suspected of Huntington's disease and without mutation in the IT15 gene.
2008
·
Anna Sułek-Piatkowska
, Wioletta Krysa
, et al.
·
PubMed
·
12
CAG repeat polymorphism in the androgen receptor (AR) gene of SBMA patients and a control group.
2005
·
Anna Sułek
, Dorota Hoffman-Zacharska
, et al.
·
PubMed
·
11
Peripheral nerve involvement in myotonic dystrophy type 2 – similar or different than in myotonic dystrophy type 1?
2015
·
Monika Nojszewska
, Anna Łusakowska
, et al.
·
Neurologia i Neurochirurgia Polska
·
10
Screening for premutation in the FMR1 gene in male patients suspected of spinocerebellar ataxia.
2009
·
Marta Rajkiewicz
, Anna Sułek-Piatkowska
, et al.
·
PubMed
·
10
The needle EMG findings in myotonia congenita
2019
·
Monika Nojszewska
, Anna Lusakowska
, et al.
·
Journal of Electromyography and Kinesiology
·
8
PDF
Value of short exercise and short exercise with cooling tests in the diagnosis of myotonic dystrophies (DM1 AND DM2)
2013
·
Malgorzata Gawel
, Elzbieta Szmidt‐Salkowska
, et al.
·
Muscle & Nerve
·
8
Does quantitative EMG differ myotonic dystrophy type 2 and type 1?
2014
·
Elzbieta Szmidt-Salkowska
, Malgorzata Gawel
, et al.
·
Journal of Electromyography and Kinesiology
·
7
A molecular and cytogenetic investigation of FMR1 gene premutations in Polish patients with primary ovarian insufficiency
2011
·
Marta Rajkiewicz
, Katarzyna Szlendak-Sauer
, et al.
·
European Journal of Obstetrics & Gynecology and Reproductive Biology
·
4
Clinical evaluation of the effectiveness of teleneuroforma – A home rehabilitation tool for patients with Huntington's disease
2019
·
K. Ziora-Jakutowicz
, M. Rakowicz
, et al.
·
Journal of the Neurological Sciences
·
3
PDF
Hereditary form of prion disease in Poland
2012
·
Janusz Zimowski
, Jerzy Kulczycki
, et al.
·
Neurologia i Neurochirurgia Polska
·
3
Evidence for a relatively high proportion of DM2 mutations in a large group of Polish patients
2018
·
Anna Sulek
, Anna Lusakowska
, et al.
·
Neurologia i Neurochirurgia Polska
·
1
Frequently observed polyneuropathy expands phenotypic spectrum of apparently pure autosomal dominant hereditary spastic paraplegias
2025
·
Iwona Stępniak
, Maria Rakowicz
, et al.
·
Neurologia i Neurochirurgia Polska
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Works count:
42
Citation count:
1,138
H-index:
13
I10-index:
17
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